Evidence map›Paper›PMID 35366281›Full record

ArticlePathophysiology : the official journal of the International Society for Pathophysiology2021

Neuroendocrine Tumors: Clinical, Histological and Immunohistochemical Perspectives and Case Report-Mature Teratoma in a 16-Year-Old Girl.

Elżbieta Sowińska-Przepiera, Dariusz Starzyński, Anhelli Syrenicz, Ireneusz Dziuba, Barbara Wiszniewska, Sylwia Rzeszotek

Open access · goldAbstract readCase Reports
In one paragraph

Article in Pathophysiology : the official journal of the International Society for Pathophysiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 48% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Elżbieta Sowińska-PrzepieraDepartment of Endocrinology, Metabolic and Internal Diseases, Pomeranian Medical University (PMU), 71-252 Szczecin, Poland.
Dariusz StarzyńskiDepartment of Endocrinology, Metabolic and Internal Diseases, Pomeranian Medical University (PMU), 71-252 Szczecin, Poland.
Anhelli SyreniczDepartment of Endocrinology, Metabolic and Internal Diseases, Pomeranian Medical University (PMU), 71-252 Szczecin, Poland.
Ireneusz DziubaFaculty of Medicine, University of Technology, 40-555 Katowice, Poland.ORCID 0000-0001-5399-9645
Barbara WiszniewskaDepartment of Histology and Embryology, Pomeranian Medical University (PMU), 70-111 Szczecin, Poland.
Sylwia RzeszotekDepartment of Histology and Embryology, Pomeranian Medical University (PMU), 70-111 Szczecin, Poland.ORCID 0000-0002-2157-0315
Pomeranian Medical University · PLAkademia Śląska · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A mature teratoma is a germinal neoplasm that differentiates from embryonic multipotent cells into three germ layers. There may also be glandular tissue. The literature describes a total of 658 cases of ovarian neuroendocrine neoplasms, mainly in women over 40 years of age. The authors, together with a systemic review, present a case of a 16-year-old girl diagnosed with and treated for a neuroendocrine tumor. Case description: A 16-year-old girl visited the Paediatric Gynaecology Outpatient Clinic because of abdominal pains that intensified during menstruation. Standard painkillers and diastolic drugs were ineffective. An ultrasound examination revealed a large tumor with a heterogeneous structure in her right ovary. A sparing operation was carried out. During laparotomy, the lesion was enucleated, leaving healthy tissue. Histopathological examination revealed the typical features of teratoma, as well as the coexistence of a G1 neuroendocrine tumor. Immunohistochemical examination (IHC) showed the presence of markers characteristic for this type of tumor. The patient requires constant monitoring in the Endocrinology and Oncological Gynaecology Clinic. Conclusion: Tissue of neuroendocrine neoplasm within a teratoma is rare in this age group of patients; thus, there are currently no standards for long-term follow-up. This case adds to the body of evidence and demonstrates a possible good prognosis with non-aggressive behavior in G1 neuroendocrine tumors and teratomas in young patients.

Indexed as

germinal neoplasmIHCneuroendocrine tumorovarian tumorpediatric gynecologyteratoma

Identifiers

PMID35366281
PMCPMC8830444
OpenAlexW3198060367

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.